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Highlighted Tests
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why choose ambry
Ambry places significant value on implementing new lab processes designed to increase quality, and advancing technology across the field with innovative approaches. Our ongoing participation in numerous research studies and collaborations is so that we can better assess clinical validity of gene-disease relationships. This is to ensure that the results healthcare providers receive are as accurate and informative as possible. That’s why we led the largest study of its kind (20,000 cases) guiding us on additional confirmatory testing when we saw specific well-defined thresholds, reducing the chance of delivering a false positive patient report or one that misses real mutations (Mu et al., November 2016). The more accurate the reports, the more insight healthcare providers will have to treat their patients.
Choose from one of our more frequently ordered tests listed below.
CancerNext®
CancerNext is a guideline-based, pan-cancer test that includes 39 genes associated with the most common hereditary cancer types, including hereditary breast, ovarian, pancreatic, prostate, colorectal/polyps, endometrial, gastric, small bowel, urothelial, and renal cancers.
CancerNext-Expanded®
As Ambry’s most comprehensive, pan-cancer test option for hereditary cancer predisposition, CancerNext-Expanded includes up to 90 genes associated with a wide range of hereditary cancers such as breast, ovarian, uterine, colorectal, gastric, pancreatic, prostate, melanoma, renal, central nervous system tumors, pheochromocytoma/paraganglioma, hematologic malignancy, and other rare cancer predisposition conditions.
BRCAplus®
BRCAplus is a guideline-based, disease-specific test option that includes 13 genes associated with hereditary breast cancer, where screening and/or surgical intervention may be indicated.
BRCANext®
BRCANext is a guideline-based, disease-specific test option that includes up to 26 genes associated with hereditary breast and/or gynecologic cancers.
ColoNext®
ColoNext is a guideline-based, disease-specific test option that includes up to 26 genes associated with hereditary colorectal and gastric cancer and polyposis.
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Comprehensive
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Comprehensive Testing
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Comprehensive
Comprehensive Testing
Name TAT Genes CancerNext® 14-21 days 39 CancerNext-Expanded® 14-21 days 76
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Customizable Testing
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Comprehensive
Customizable Testing
Name TAT Genes CustomNext-Cancer® 14-21 days 90
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Comprehensive Testing
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Breast + Gynecological
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For risk assessment of multiple hereditary cancers
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Breast + Gynecological
For risk assessment of multiple hereditary cancers
Name TAT Genes CancerNext® 14-21 days 39 CancerNext-Expanded® 14-21 days 76
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For patients with a personal/family history of breast cancer
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Breast + Gynecological
For patients with a personal/family history of breast cancer
Name TAT Genes BRCAplus® 7-10 days 13
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For patients with a personal/family history of breast cancer and/or gynecological cancer
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Breast + Gynecological
For patients with a personal/family history of breast cancer and/or gynecological cancer
Name TAT Genes BRCANext® 14-21 days 19
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For risk assessment of multiple hereditary cancers
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Gastrointestinal
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For risk assessment of multiple hereditary cancers
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Gastrointestinal
For risk assessment of multiple hereditary cancers
Name TAT Genes CancerNext® 14-21 days 39 CancerNext-Expanded® 14-21 days 76
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For patients with a personal/family history of gastrointestinal cancer and/or polyps
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Gastrointestinal
For patients with a personal/family history of gastrointestinal cancer and/or polyps
Name TAT Genes ColoNext® 14-21 days 20
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For risk assessment of multiple hereditary cancers
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Single Gene
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Single Gene
Single gene or single syndrome testing options
Name TAT APC gene sequence and deletion/duplication analysis 14-21 days ATM gene sequence and deletion/duplication analysis 14-21 days BAP1 gene sequence and deletion/duplication analysis 14-21 days BRCA1/BRCA2 gene sequence and deletion/duplication analysis 6-10 days BMPR1A/SMAD4 gene sequence and deletion/duplication analysis 14-21 days CDH1 gene sequence and deletion/duplication analysis 14-21 days CDKN2A/CDK4 gene sequence and deletion/duplication analysis 14-21 days CHEK2 gene sequence and deletion/duplication analysis 14-21 days DICER1 gene sequence and deletion/duplication analysis 14-21 days EPCAM deletion/duplication analysis 7-14 days FH gene sequence and deletion/duplication analysis 14-21 days FLCN gene sequence and deletion/duplication analysis 14-21 days MEN1 gene sequence and deletion/duplication analysis 14-21 days MITF specific site analysis 7-14 days MLH1 gene sequence and deletion/duplication analysis 14-21 days MSH2 gene sequence and deletion/duplication analysis, MSH2 inversion analysis, and EPCAM deletion/duplication analysis 14-21 days MSH6 gene sequence and deletion/duplication analysis 14-21 days MUTYH gene sequence and deletion/duplication analysis 14-21 days NF1 gene sequence and deletion/duplication analysis 14-21 days NF2 gene sequence and deletion/duplication 14-21 days PALB2 gene sequence and deletion/duplication analysis 14-21 days PMS2 gene sequence and deletion/duplication analysis 14-21 days PTCH1 gene sequence and deletion/duplication analysis 14-21 days PTEN gene sequence and deletion/duplication analysis 14-21 days RB1 gene sequence and deletion/duplication analysis 14-21 days RET gene sequence 14-21 days SMARCB1 gene sequence and deletion/duplication 14-21 days STK11 gene sequence and deletion/duplication analysis 14-21 days TP53 gene sequence and deletion/duplication analysis 14-21 days TSC1/TSC2 gene sequence and deletion/duplication analysis 14-21 days VHL gene sequence and deletion/duplication analysis 14-21 days
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